Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
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BACKGROUND OF THE IWVENTION
Collected blood may be conventionally certrifuged
to remove the plasma and the buffy coat layer, leaving be-
hind the "packed red cells", as the mass of red cells is
substantially separated from the plasma. This i5 desirable
for several reasons, first to collect the plasma for separ-
ate therapeutic use, but also because it is desirable to
administer concentrated red cells during major surgery, to
provide the patient with a maximum amount of red cells with
a minimum of added fluids, to avoid overburdening the pat-
ient's vascular system with excess fluids.
Accordingly, it is deemed desirable in many forms
of medical practice and blood banking to store the packed
red cells separately, apart from a substantial portion of
the plasma, for later administration to a patient during
major surgery or the like, while the collected plasma finds
a separate medical use, for example administration to ano-
ther patient or processing into various medical components
such as antihemophilic factor, and plasma protein fraction.
However, it was discovered that packed red cells
did not survive as well as red cells which were not packed
(i.e., those which were stored in the presence of more
plasma).
To promote the long term storage of packed red
cells, it has been previously suggested to admix with a
unit of packed red cells (which is typically about 225 ml
of packed cells but is, of course, subject to variation
according to the individual donor) a small amount labout
lO0 ml) of blood plasma.
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In a major contribution in this area, Dr. Claes
F. Hogman of Sweden observed that storing packed red
cells in a protein-poor soiution containing, for each
unit of packed red cells, 877 mg of sodium chloride,
16.9 mg of adenine, and 900 mg of glucose (hereafter
SAG) increased the storage period of the cells. See,
for example, Hogman, et al, The New England Journal of
Medicine, December 2i, 1978; 229(25); 1377-82. Another
protein-poor medium for packed red cells is reported
by Loveric, et al, ~edical Journal of Australia, 1977,
2:183-186.
It has also been suggested to use mannitol, which
is a type of sugar, as a reagent to improve the via-
bility of stored blood cells. However, surprisingly,
it has been found in accordance with this invention
that despite the fact that SAG solution contains abun-
dant sugar already, the addition of mannitol provides
a significant improvement in the viability of packed
red cells stored in contact therewith. Accordingly,
longer storage times appear to be possible for packed
red cells with better viability than has been previous-
ly available.
DESCRIPTION OF THE INVENTION
In accordance with an aspect of this invention,
an aqueous red cell storage solution is provided, par-
ticularly for admixture with highly concentrated or
packed red cells, for improving the viability of the
cells upon storage. The solution contains, per 100 ml.,
essentially from 5 to 50 mg. of adenine; from 1000 to
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3500 mg. of a sugar such as glucose or fructose;
from 400 to 1200 mg. of sodium chloride; and from 250
to 2000 mg. of mannitol.
In accordance with another aspect of this
invention there is provided a unit of red blood cells,
intermixed with from 60 to 200 ml. of an aqueous red cell
storage solution which contains, per 100 ml. of said
storage solution, essentially from 5 to 50 mg. of adenine;
from 1000 to 3500 mg. of a sugar selected from the group
consisting of glucose and fructose; from 400 to 12Q0 mg.
of sodium chloride, and from 250 to 2000 mg. of mannitol.
Preferably, per 100 ml. of solution, from 20 to
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30 mg. of adenine, from 1500 to 2500 mg. of glucose or fruc-
tose, from 500 to 1000 mg. of sodium chloride, and from 500
to 1500 mg. of mannitol are present. Particularly, from
700 to 800 mg. of mannitol may be present per 100 ml. of
solution, for example, 750 mg.
A specifically preferred solution in accordance
with this invention may contain, per 100 ml., about 27 mg.
of adenine, 2000 mg. of glucose, 900 mg. of sodium chloride
and 750 mg. of mannitol, these solutes being carefully dis-
solved in distilled water and then sterilized and sealed
in conventional manner.
For example, a conventional triple or quadruple
pack blood bag of conventional design for receiving one unit
of blood, comprising a donor bag and two or three satellite
transfer bags or packs may be utilized, with typically about
60 to 200, and preferably 80 to 150 ml., of the above spe-
cifically described solution being placed in one of the trans-
fer bags. Preferably an extra interior seal, openable from
the exterior, is provided to the connecting tube between the
solution-containing transfer bag and the donor bag adjacent
the transfer bag, for example, the CELL-PROOF~ closure of
the Fenwal Division of Baxter Travenol Laboratories, or the
closure of U.S. Patent No. 4,181,140.
A unit of blood may be accordingly collected in
conventional manner into the donor bag. The three or four
bag system may be conventionally centrifuged, and the plasma
- and buffy coat layer can be expressed-into an empty trans-
fer bag by appropriate manipulation of the clamping and in-
ternal sealing system provided by the bag system. The red
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cell storage solution in the first transfer pack may then be
expressed into the donor bag, and the donor bag may then be
sealed and separated from the remaining bags for long term
storage.
Following this, the plasma-containing transfer
bag may be centrifuged to separate platelets, with the plate-
let-poor plasma then being expressed from the plasma-contain- -
ing transfer bag into the transfer pack which formerly con-
tained red cell storage solution in the case of a triple bag.
The transfer packs may be then separated for separate stor-
age and therapeutic administration or other use as desired.
The fourth bag of a multiple bag unit may be provided to re-
ceive the leucocytes, for example.
Long-term storage of packed red cells at 4C. under
conventional storage conditions for 35 days and more is possi-
ble, with the red cells exhibiting improved viability in ac-
cordance with this invention.
Preferably, the donor bag contains a usual amount
of CPD preservative. Also, the solution of this invention
may contain other ingredients as desired, for example, guano-
sine, or phosphate, calcium, magnesium or potassium ion, etc.
The following example is offered for illustrative
purposes only, and is not intended to limit the invention of
this application, which is as defined in the claims below.
Example. A triple bag system of the conventional
design of the Fenwal BLOOD-PACK~ system, containing a donor
bag with CPD preservative of the usual type, and two trans-
fer bags were utilized in this experiment, but also con-
taining an added inner seal at the first transfer bag, open-
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able from the exterior, in the tube leading between the donor
bag and the transfer bag. I~ere indicated, the first trans-
fer bag contained 100 ml. of the cell diluent solution des-
cribed below. In each experiment a unit of blood was collected
5 in the donor bag, centrifuged, and the plasma was expressed
from the donor bag to the second transfer bag. Then, the 100
ml. of solution in the first transfer bag was expressed into
the donor pack, which was then sealed, separated from the bag
system, and stored for 35 days at 4C. in conventional manner.
Referring to experiments (a) through (e) as des-
cribed below, in experiment (a), the 100 ml. of solution in
the first transfer bag was simply saline solution containing
900 mg. of sodium chloride per 100 ml.
In experiment (b), no diluent solution at all was
used, with the packed cells being stored in their undiluted
configuration.
In experiment (c), the packed cells were diluted
with 100 ml. of plasma, which was simply re-expressed back
to the cells from the second transfer bag containing the
plasma.
In experiment (d) below, the 100 ml. of solution
placed in the transfer pack contained 1000 mg. of glucose,
approximately 17 mg. of adenine, and about 800 mg. of sodium
chloride. No mannitol was present.
In experiment (e) below, the 100 ml. of solution
in the first transfer pack was an embodiment of the solution
of this invention, containing 27 mg. of adenine; 2000 mg.
of glucose; approximately 500 mg. of sodium chloride; and
750 mg. of mannitol.
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After processing of the blood in accordance with
the technique described above, each of the donor bags of the
five experiments (a) through (e) were stored at 4C. for 35
days.
At the conclusion of the 35 days, the plasma hemo-
globin was measured in terms of mg. per 100 ml., and the red
cell ATP was measured and expressed in Table I below as micro-
moles per gram of red cell hemoglobin.
TABLE I
PLASMA
TREATMENT CO~DITIONS HEMOGLOBIN ATP (Micromoles/g.
10PRIOR TO STORAGE (mg./100ml.) Red Cell Hemoglobin)
(a) packed cells with
saline solution r.lore than 1000 about 1.5
~b) packed cells only more than 1000 about 2.5
(c) packed cells plus
100 ml. plasma 200 about 1.75
(d) saline, adenine,
glucose solution
without mannitol 500 about 4
(e) the solution of
this invention con-
15taining mannitol 180 about 5
Accordingly, it can be seen that in accordance with
this invention, substantially decreased plasma hemoglobin
levels, and significantly increased ATP levels are achieved on
35 day storage of packed cells, when compared with prior art
20techniques.
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